Abstract: An intramedullary nail extractor including a central body, a rotatable sleeve and a clamping member. The central body includes a proximal end for attachment to an extractor, a distal end having a hook for engaging an intramedullary nail, and a threaded intermediate portion between the proximal end and the distal end. The rotatable sleeve threadedly engages the threaded intermediate portion of the central body, and the clamping member is operatively engaged by the rotatable sleeve and moveable relative to the central body.

Abstract: Knee replacement prosthesis are provided, comprising a plurality of sensors and at least one of a femoral component, a patellar prosthesis and a tibial component.

Abstract: The invention relates to a method for treating hip joint osteoarthritis with a medical device having a prosthetic part adapted to function as an articulating surface comprising a center axis generally coinciding with the acetabulum and the caput femur center axis when implanted. The method further comprises placing the prosthetic part in a through-going hole in the pelvic bone from the side opposite a concave portion of the acetabulum of the human patient, displacing at least one displaceable protruding supporting member connected to said prosthetic part such that the at least one displaceable protruding supporting member is configured to transfer load from the prosthetic part via the displaceable connection to the pelvic bone when being displaced relative said prosthetic part in a direction more perpendicular than parallel to the prosthetic part's center axis and being implanted.

Abstract: A system for preparing a bone for implantation of a component of an orthopedic implant device. The system includes a forming tool having a sleeve member that is selectively received within a handle member. The sleeve member has a guide slot that is sized to receive axial passage of at least a portion of a guide. The guide slot and/or sleeve member may be positioned and/or configured to facilitate at least linear and/or rotational displacement of the forming tool about, or relative to, the guide, and thereby provide a degree of freedom in the location at which the forming tool may form a shape or opening in the bone relative to one or more reference axes. The handle member may include a connection member that is structured to be operably coupled to a bone preparation device that is structured to facilitate the displacement of bone material.

Abstract: A hip/shoulder prosthesis includes: a head component; a metaphyseal component; a diaphyseal nail, and a locking device. The head component includes: a front face and rear face; with a bore, and first and second shaped recesses in the rear face. The metaphyseal component includes: a central transverse aperture at an angle to the metaphyseal component's axis; a first end configured for threaded engagement within the bore of the head component; and a longitudinal hole that begins at the second end, transects the transverse aperture and reaches the first end, to receive the locking device. The diaphyseal nail is inserted in the femoral or humeral canal, and includes: fastening apertures that receive corresponding screws for fastening the diaphyseal nail to the femur or humerus; a portion configured to be received within, and engage, the transverse aperture of the metaphyseal component, and a transverse hole configured to receive the locking device.

Abstract: Disclosed herein is a device that helps to reduce the potential for inaccuracies and uncertainties associated with allograft cartilage transfer procedures. In one embodiment, the disclosed device generally includes a shaft, a stationary ring attached to the shaft, and a movable ring attached to the shaft and configured to move either toward the stationary ring or away from the stationary ring along the axis of the shaft. In practice, the device may be placed within a recipient cavity and adjusted such that one ring is positioned at the distal surface of the recipient cavity and the other ring is flush with the native cartilage surface of the recipient. The device may be removed from the recipient cavity, a donor graft placed within, and any excess donor graft extending beyond the rings trimmed off. The donor graft may then be removed from the device and inserted within the recipient cavity.

Abstract: A method of preparing a surgical site includes the steps of: disposing a preparation material with a selected surface of a patient body, the selected surface includes a sterile region having a boundary; engaging a first applicator with the selected surface and moving the first applicator along a path from a first incision site of the selected surface to the boundary; engaging a second surgical applicator with the selected surface and moving the second applicator along a path from a second incision site of the selected surface to the boundary, the path of the first applicator intersecting the path of the second applicator. In some embodiments, surgical systems and surgical instruments are disclosed.

Abstract: The present disclosure includes, in one embodiment, a talar component of an ankle joint prosthesis for engagement with a talus bone having a medial side wall and a lateral side wall, opposite the medial side wall, each side wall terminating at a distal edge, and the distal edges adapted to drive into the talus bone. When implanted, the side walls may form a seal between the talus bone and the component to prevent fluid from flowing under the component.

Abstract: The present inventions relate to devices and methods that improve the positioning and fit of orthopedic reconstructive joint replacement stem implants relative to existing methods. For example, an embodiment of the device provides a stem component comprising proximal and distal body portions that can be configured to mimic a geometric shape of a central cavity region created in a bone of a joint for improving conformance and fixation of the stem component thereto. Further, another embodiment provides a system of stem implants that each have a unique medial offset for facilitating the matching of an implant to the geometry of a central cavity region of a bone. Additionally, an inclination angle of a resection surface of each of the implants in the system can remain constant or vary as a function of the medial offset.

Abstract: The present invention relates to a method of providing a graft scaffold for cartilage repair, particularly in a human patient. The method of the invention comprising the steps of providing particles and/or fibres; providing an aqueous solution of a gelling polysaccharide; providing mammalian cells; mixing said particles and/or fibres, said aqueous solution of a gelling polysaccharide and said mammalian cells to obtain a printing mix; and depositing said printing mix in a three-dimensional form. The invention further relates to graft scaffolds and grafts obtained by the method of the invention.

Abstract: Femoral heads, mobile inserts, acetabular components, and modular junctions for orthopedic implants, e.g., hip replacement implants, and methods of using femoral heads, mobile inserts, acetabular components, and modular junctions for orthopedic implants are provided. Prosthetic femoral heads, mobile inserts, and acetabular components are provided that can alleviate soft tissue impingement, reduce implant wear, and/or reduce frictional torque. Modular junctions are provided that can minimize the incidence of loosening and micromotion that can occur at modular junctions of orthopedic implants.

Abstract: An adjustable humeral implant includes a humeral tray and a humeral coupler. The humeral tray includes a humeral coupler receiving portion. The humeral coupler includes a humeral tray mating portion and a stem portion extending from the humeral tray mating portion along a first axis. The humeral tray mating portion is translatable within the humeral coupler receiving portion in a direction transverse to the first axis.

Abstract: Femoral heads, mobile inserts, acetabular components, and modular junctions for orthopedic implants, e.g., hip replacement implants, and methods of using femoral heads, mobile inserts, acetabular components, and modular junctions for orthopedic implants are provided. Prosthetic femoral heads, mobile inserts, and acetabular components are provided that can alleviate soft tissue impingement, reduce implant wear, and/or reduce frictional torque. Modular junctions are provided that can minimize the incidence of loosening and micromotion that can occur at modular junctions of orthopedic implants.

Abstract: A hip implant having two distinct bodies, a neck body and a bone fixation body. The neck body is formed from a solid metal and has an interface for connecting to a femoral ball. The bone fixation body has an elongated shape and is formed as a porous structure that is inserted into an intramedullary canal of a patient.

Abstract: A method of performing joint arthroplasty on a patient with a bone fragment of a bone at least partially separated from the bone in one embodiment includes providing a prosthetic component with a bone connecting portion and a bone fragment portion, implanting the bone connecting portion of the prosthetic component in the bone, and attaching the bone fragment to the bone using the bone fragment portion.

Abstract: A spacer device (1) for the two-step treatment of prosthesis infections, made from biologically compatible and porous material designed to allow the possibility of adding pharmaceutical products, active and/or therapeutic ingredients, includes a first portion (2) designed to be fixed to a corresponding bone bed remaining from a previous implant, and a second portion (3) designed to be inserted in a corresponding articular area of the patient, the first portion (2) and the second portion (3) being attached by adjustable connecting means (4).

Abstract: A method for performing an orthopaedic surgical procedure on a femur includes attaching a proximal end of an intramedullary adaptor to an intramedullary orthopaedic surgical instrument, securing a distal end of an intramedullary adaptor to a base cutting block, inserting the intramedullary orthopaedic surgical instrument into a medullary canal using the base cutting block, and positioning the base cutting block on a distal end of the femur.

Abstract: An orthopaedic surgical instrument assembly includes a base block, an intramedullary orthopaedic surgical instrument configured to be inserted into a medullary canal of a patient's femur, an adaptor, and a modular cutting block. The base cutting block includes a slot, and the adaptor is positioned in the slot. The adaptor includes a mounting bracket engaged with the base plate, and a fastener coupled to the intramedullary orthopaedic surgical instrument. The modular cutting block is configured to be secured to the base block.

Abstract: Methods and apparatuses for attaching tissue structures to orthopaedic implants. In one exemplary embodiment, the methods and apparatuses are used to attach soft tissue and/or bone to a proximal tibial implant. In another exemplary embodiment, the methods and apparatuses are used to attach soft tissue and/or bone to a proximal femoral implant.

Abstract: Methods and apparatus for orthopedic replacement of the hip and hip fracture fixation devices include structures and techniques for fixing or enhancing interconnection of implant components, such as by increasing the interconnection in an interference fit with one or more tapers, threads, and/or cooling of components prior to assembly. For example, a prosthetic femoral neck implant can include a thread and a Morse taper for lockable attachment to a prosthetic femoral head and/or intramedullary stem.

Abstract: Disclosed is an orthopedic implant that includes an anchor, a bore, and a compressible and expandable mesh. The anchor is configured to secure the implant at an implantation site and defines a longitudinal axis. The bore is defined by the anchor and extends along the longitudinal axis. The compressible and expandable mesh is aligned along the longitudinal axis and defines a plurality of openings. The mesh is configured to compress along the longitudinal axis and expand from the longitudinal axis to engage surrounding bone or tissue at the implantation site to secure the implant at the implantation site.

Abstract: A prosthetic femoral implant for use in a hip joint, as a ball and socket type joint, is disclosed. The implant includes a modular neck having a variety of adjustable positions to adjust the lateral offset and version angle of the femoral implant in relation to the femur. The implant further includes a broad, full collar for providing a compression force increasing the interdigitation between the interface of the bone, implant and cement. The implant also includes a stem having a depression having a roughened porous surface for resisting the increased torsional loads placed on the implant due to the increased lateral offset and version angle. The stem further comprises three distinct zones, each zone having its own roughened surface creating a tripartite differential porosity.

Abstract: A femoral prosthesis for use during performance of a hip replacement procedure includes a plurality of femoral stem components in a range of various sizes and a plurality of femoral head component in a range of various sizes. The anterior/posterior stem taper angle of the femoral stem component varies across its range of sizes.

Abstract: Hip replacement surgery (hip arthroplasty) includes implantation of a distal stem into a femur of a patient, and implantation of a proximal body to connect to the distal stem. A practitioner uses a “trial” or “provisional” to determine a suitable size and configuration for the implantable proximal body, then selects a suitable proximal body from a set of differently sized and shaped proximal bodies. The trial adjusts discretely, as opposed to continuously, and has discrete settings that correspond to the sizes and configurations available in the set of implantable proximal bodies. In some examples, the trials are provided as a kit of parts, where each part in the kit is adjustable for height (i.e., the length of the femur). The parts in the kit can have different, fixed, values for offset (i.e., the lateral distance of the femur to the center of the femoral head in the acetabulum).

Abstract: A method of orienting a femoral head member of an implant relative to an acetabular member positioned in the acetabulum including implanting a femoral stem of an implant within an intramedullary canal of a femur, inserting an acetabular member in the acetabulum, positioning a femoral head member of the implant at least partially in the acetabular member with the femoral head member including a curved articulating surface and a plurality of indicia on the curved articulating surface, and orienting the femoral head member relative to the acetabular member and generally aligning one of the indicia on the curved articulating surface with an alignment feature of the acetabular member to signify an orientation of the femoral head member relative to the acetabular member.

Abstract: A method for centering a stem of an implant at an implantation site. The method includes implanting at the implantation site the implant having a sleeve rigidly mounted to the stem of the implant, the stem extends through an interior area of the sleeve. The method further includes compressing the sleeve by applying force to the sleeve to expand a mesh portion of the sleeve outward from the stem and into engagement with sidewalls of the implantation site to thereby center the stem at the implantation site.

Abstract: For replacing a human hip or knee joint and the adjoining bone sections, an implantable prosthesis is provided, comprising a joint replacement part (10), a shaft replacement part (12) and a rod-shaped shaft anchoring part (16) being insertable into an axial cavity (14) in the shaft replacement part (12).

Abstract: A method of forming an orthopedic implant, the method comprising the steps of providing a first implant component and a second implant component, the first implant component having a stem and a second implant component including a head defining a female taper sized to receive the stem; coupling the stem to the female taper of the head; forming a modular injunction between the stem and head; applying a seal to the modular injunction to limit bodily fluid from contacting the modular injunction; and forming the orthopedic implant.

Abstract: Orthopedic hip replacement is made safer and more effective by enhancing interconnection of hip implant components, such as by improving an interference fit using one or more tapers, threads, and/or cooling of components prior to assembly. For example, a prosthetic femoral neck can include a thread and a Morse taper for lockable attachment to a prosthetic femoral head and/or intramedullary stem. A monoblock head and neck unit is described, having an integrated prosthetic femoral head and prosthetic neck, with structures for engaging the stem.

Abstract: The present teachings are directed to a shoulder prosthesis having an adjustable radial offset and/or angular inclination provided by relative rotation of an adapter interdisposed between a stem and a head. In one example, a prosthesis has a stem having a first longitudinal axis. The prosthesis can also include an adaptor including a first taper. The first taper can have a first taper axis. The prosthesis can include a head supported by the adaptor. The head can be selectively oriented and then coupled to the first taper and the combination can be selectively orientated and the coupled to the stem.

Abstract: A hip arthroplasty prosthesis for treating a patient condition includes a stem portion configured to penetrate into the bone of a femur of the patient, and includes a head portion formed of a polymeric material and being fixedly attached to the stem portion. The head portion may include a spherical portion with a diameter sized to match the diameter of an acetabulum of an adult patient in a manner permitting the acetabulum to interface with and articulate relative the head portion over a distributed portion of the head portion.

Abstract: A femoral hip implant includes a first end, a second end, and a collar with a porous surface, all fabricated from a single piece of material. The entire area of the collar is porous, and the collar elastically deflects under load to promote bone ingrowth.

Abstract: The present disclosure provides a femoral prosthesis for use during a revision procedure. The femoral prosthesis includes a body, a neck, a stem, and a sleeve. The sleeve facilitates reattachment of an osteotomized proximal femur, specifically the greater trochanter, following a revision femoral prosthesis surgery involving an extended trochanteric osteotomy. Additionally, the sleeve promotes ingrowth of the osteotomized proximal femur with the sleeve.

Abstract: The present disclosure provides a femoral prosthesis for use during a revision procedure. The femoral prosthesis includes a body, a neck, a stem, and a sleeve. The sleeve facilitates reattachment of an osteotomized proximal femur, specifically the greater trochanter, following a revision femoral prosthesis surgery involving an extended trochanteric osteotomy. Additionally, the sleeve promotes ingrowth of the osteotomized proximal femur with the sleeve.

Abstract: A prosthetic femoral component comprising: (a) a femoral shaft; (b) a femoral neck operatively coupled to the femoral shaft; and, (c) a femoral ball operatively coupled to the femoral shaft, where a neck axis extending longitudinally through the femoral neck is angled at no greater than thirty-five degrees with respect to a femoral shaft axis extending longitudinally through the femoral shaft.

Abstract: Methods for performing a hemiarthroplasty procedure. In some implementations, the method may comprise providing a component of an endoprosthesis, such as a femoral component of a hip prosthesis. The component may comprise a silicon nitride ceramic material, and may further comprise a coated articulating surface. The coated articulating surface may comprise a coating configured to reduce a coefficient of friction of the articulating surface. The method may further comprise positioning the endoprosthesis such that the coated articulating surface is positioned adjacent to a patient's native articular cartilage. In this manner, the coated articulating surface may articulate with the native articular cartilage following the procedure.

Abstract: A porous coating for a medical implant, wherein the porous coating comprises a porous, shape memory material.

Abstract: A ready-for-use polymer cement spacer device for the replacement of a permanent joint prosthesis during a two-stage replacement, includes a shank includes for attachment for placing to the supporting bone and a head in the joint region. The spacer device includes two complementary members incorporating rigid members for assembly between them, the first member being loaded with a first active substance and the second member being loaded with a second active substance. The first and second active substances are preferably antibiotics, selected from gentamycin, trobamycin, vancomycin, erythromycin, fucidin, tetracycline or other suitable antibiotics. The temporary joint implant maintains a suitable space for the time necessary for the operation of replacing a permanent prosthesis to prevent tissues from occupying the space released by removal of the permanent prosthesis and ensures effective treatment of resistant infections by local treatment of the joint area through at least two different active substances.

Abstract: The invention reduces friction and wear in partial hip prosthesis by combining optimized geometry of the articulation and surface treatment of the prosthetic component. The acetabulum is reamed to the bone. One of the articulating surfaces—either that of the reamed acetabulum, or that of the femoral head prosthesis is a-spherical so that a fluid-filled gap is formed at the area of major load transfer. The fluid-filled gap is sealed by an annular area of contact, over which the concave and the convex components are congruent. The preferred surface treatment is by diamond-like coating, which results in very low coefficient of friction and high abrasion resistance against the bone. The prosthetic head is fixed to the femur by either a conventional stem, a perforated shell, or a femoral neck prosthesis screwed onto the femur so that it is partially covered by bone and partially exposed on the medial-inferior aspect, where it abuts the reamed cortex of the calcar region.

Abstract: Provided herein are hip implant devices and related surgical methods. The hip implants and methods can optionally be used in patients of Asian descent.

Abstract: An implant includes a body configured to be implanted at least partially within a bone canal. The body has a proximal end, a longitudinal axis and a cavity located at the proximal end. The cavity is configured to mate with an insertion tool and defines a cavity axis that is not parallel to the longitudinal axis of the implant.

Abstract: A device and method for the stabilization of the shafts of threaded hip pins in the treatment of intracapsular fractures of the neck of the femur, using an intertrochanteric hip pin stabilizing rod, a cortical side plate with a releasably attached drill and insertion tool jig, said jig comprising a means for accurately inserting said rod and a plurality of parallel threaded hip pins through openings in the jig, the cortical side plate, and the intertrochanteric pin stabilizing rod, across the fracture and into the head of the femur.

Abstract: Methods and apparatus of the present invention provide for orthopaedic replacement of the hip while substantially preserving muscles and soft tissues around the hip joint resulting in reduced healing time and decreased risk of dislocation following the procedure. In an exemplary embodiment, an intramedullary rod 1502 is inserted longitudinally into the femur. A prosthetic femoral neck 3102 is then inserted from a point along the side of the patient's body and into the side of the femur and through a pre-existing lateral bore in the intramedullary rod 1502 and through the remainder of the femur to join the prosthetic femoral head 1102. The methods and apparatus include structures and techniques for fixing the prosthetic femoral neck 3102 in relation to the intramedullary rod 1502.

Abstract: A femoral stem including a stem member having a distal part of the stem member which is inserted in a medullary cavity of a femur and fixed therein and a proximal part of the stem member which has a neck for fixing an artificial head and is positioned at a proximal end of the distal part. The distal part and the proximal part are integrated or separable. Also, a plate fixing portion is detachably attached at a top of the proximal part, and a greater trochanter plate is provided for depressing the greater trochanter. The greater trochanter is fixed to the plate fixing portion at a certain angle or is fixed to the plate fixing portion so as to adjust an angle of the trochanter plate.

Abstract: For replacing a human hip or knee joint and the adjoining bone sections, an implantable prosthesis is provided, comprising a joint replacement part (10), a shaft replacement part (12) and a rod-shaped shaft anchoring part (16) being insertable into an axial cavity (14) in the shaft replacement part (12).

Abstract: A hip joint prosthesis adapted to be implanted in a hip joint of a human patient is provided. The hip joint prosthesis comprises a first area and a second area, and wherein said first area comprises a first material adapted to be elastic and said second area comprises a second material adapted to be elastic, and wherein said first material is adapted to be more elastic than said second material.

Abstract: Methods and apparatus for orthopedic replacement of the hip through three incisions with a modular prosthetic system assembled in vivo while substantially preserving muscles and soft tissues around the hip joint resulting in reduced healing time and decreased risk of dislocation. A prosthetic femoral stem is inserted into the femur. A prosthetic femoral neck is inserted from a point along the side of the patient's body and into the side of the femur and through a lateral bore in the prosthetic femoral stem to join the prosthetic femoral head. The methods and apparatus include structures and techniques for fixing or enhancing interconnection of implant components, such as by increasing the interconnection in an interference fit with one or more tapers, threads, and/or cooling of components prior to assembly.

Abstract: A medical device for implantation in a hip joint of a patient is provided. The hip joint has a caput femur integrated with a collum femur having a collum and caput center axis, extending longitudinal along the collum and caput femur,in the center thereof. The medical device comprises an elongated portion adapted to at least partially replace the collum femur. The elongated portion is adapted to be connected to a prosthetic spherical portion adapted to replace the caput femur. The prosthetic spherical portion in turn is adapted to be movably placed in a prosthetic replacement for the acetabulum comprising at least one extending portion adapted to clasp said prosthetic spherical portion. The elongated portion comprises a restricting portion adapted to restrict the motion range of the spherical portion in relation to said prosthetic replacement for the acetabulum.

Abstract: An implant, comprising: a head having a central axis; and a stem having a stem axis, wherein the head central axis and the stem axis are not co-linear. A method for resurfacing a femoral head, comprising the steps of: providing an implant according to the present invention; and implanting the implant with reference to the centre of the femoral neck.

Abstract: A modular hip joint implant and associated method. The modular hip implant includes a femoral stem having a proximal surface defining a dovetail groove having first and second female wings, and a neck component having a distal surface defining a semi-dovetail projection engaging the dovetail groove. The projection includes a single male wing mating with the first femoral wing.